A simple and effective approach for detecting maternal cell contamination in molecular prenatal diagnosis
Author:
Publisher
Wiley
Subject
Genetics(clinical),Obstetrics and Gynaecology
Reference35 articles.
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4. Molecular basis of myotonic dystrophy: Expansion of a trinucleotide (CTG) repeat at the 3′ end of a transcript encoding a protein kinase family member
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1. Experience in prenatal genetic testing and reproductive decision-making for monogenic disorders from a single tertiary care genetics clinic in a low-middle income country;BMC Pregnancy and Childbirth;2023-06-10
2. Experience in Prenatal Genetic Testing and Reproductive Decision-Making for Monogenic Disorders from a Single Tertiary Care Genetics Clinic in a Low-Middle Income Country;2022-11-22
3. Five Variable Number of Tandem Repeats Loci (D17S5, APOB, TPO Intron 10, IL-1α Intron 6, and CIAS1) in Thais and Application in the Prenatal Diagnostic Laboratory;Genetic Testing and Molecular Biomarkers;2022-06-01
4. Preimplantation Genetic Testing for Spastic Paraplegia Type 3;GeNeDis 2020;2021
5. Prenatal Genetic Testing for X-Linked Hypohidrotic Ectodermal Dysplasia;GeNeDis 2020;2021
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